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胆管上皮细胞的遗传谱系追踪

Genetic Lineage Tracing of Biliary Epithelial Cells.

作者信息

Rubio-Tomás Teresa, Aguilar-Bravo Beatriz, Sancho-Bru Pau

机构信息

Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.

Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Barcelona, Spain.

出版信息

Methods Mol Biol. 2019;1905:45-57. doi: 10.1007/978-1-4939-8961-4_5.

Abstract

Lineage tracing of liver cells is a powerful tool to understand liver embryonic development, healthy liver cell homeostasis, tissue repair, and regeneration. Lineage tracing of biliary epithelial cells (BECs) in the adult liver has been used to assess the contribution of the biliary epithelium to liver injury, regeneration, and disease. These studies have shown the contribution of BECs to the expansion of ductular reaction (DR) and liver progenitor cells (LPCs) and eventually the generation of new hepatocytes. Few genetic lineage-tracing mouse models have been proved to trace BECs. This chapter is focused on lineage tracing of BECs in mouse models of liver injury and regeneration. First, we mention different existing approaches to trace the biliary epithelium based on proteins specifically expressed by BECs such as sex-determining region Y-box 9 (SOX9), osteopontin (OPN), and cytokeratin-19 (KRT19). Second, we describe mouse models that can be used to evaluate cell fate during liver injury and regeneration (i.e., partial hepatectomy (PHx), acute liver injury models, and chronic liver damage models such as 3,5-diethoxycarbonyl-1,4-dihydro-collidin (DDC) diet, choline-deficient ethionine-supplemented (CDE) diet, or chronic carbon tetrachloride (CCl) administration). Third, we suggest possible readouts to assess BECs fate based on immunofluorescence analysis.

摘要

肝细胞谱系追踪是了解肝脏胚胎发育、健康肝细胞稳态、组织修复和再生的有力工具。成体肝脏中胆管上皮细胞(BECs)的谱系追踪已被用于评估胆管上皮对肝损伤、再生和疾病的作用。这些研究表明,BECs对小胆管反应(DR)和肝祖细胞(LPCs)的扩增有贡献,并最终促成新肝细胞的生成。很少有基因谱系追踪小鼠模型被证实可用于追踪BECs。本章重点介绍肝损伤和再生小鼠模型中BECs的谱系追踪。首先,我们介绍基于BECs特异性表达的蛋白质(如性别决定区Y盒9(SOX9)、骨桥蛋白(OPN)和细胞角蛋白-19(KRT19))来追踪胆管上皮的不同现有方法。其次,我们描述可用于评估肝损伤和再生过程中细胞命运的小鼠模型(即部分肝切除术(PHx)、急性肝损伤模型和慢性肝损伤模型,如3,5-二乙氧基羰基-1,4-二氢可力丁(DDC)饮食、胆碱缺乏-乙硫氨酸补充(CDE)饮食或慢性四氯化碳(CCl)给药)。第三,我们建议基于免疫荧光分析评估BECs命运的可能读数。

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